SCHEMBL5145197

SCHEMBL5145197

CC#CN(CCCC)C(=O)O

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 2/20 0.38
CA1 P00915 2/20 0.38
CA9 Q16790 2/20 0.38
MMP1 P03956 1/20 0.35
MMP2 P08253 1/20 0.35
MMP3 P08254 1/20 0.35
MMP8 P22894 1/20 0.35
AKR1B1 P15121 1/20 0.33
KDM5A P29375 2/20 0.33
KDM4C Q9H3R0 1/20 0.33
GPR84 Q9NQS5 7/20 0.32
PPARG P37231 7/20 0.32
PPARD Q03181 7/20 0.32
PPARA Q07869 7/20 0.32
HDAC11 Q96DB2 5/20 0.32
TSHR P16473 4/20 0.32
PTPN1 P18031 3/20 0.32
ALDH1A1 P00352 2/20 0.32
TLR2 O60603 2/20 0.32
TDP1 Q9NUW8 2/20 0.32

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL29664323 0.82 CA12 (0.36) CA12CA1CA9MMP1MMP2
SCHEMBL7742052 0.82 CA1 (0.36) CA12CA1CA9MMP1MMP2
SCHEMBL168928 0.79 CA12 (0.34) CA12CA1CA9MMP1MMP2
SCHEMBL1400993 0.78 CA12 (0.40) CA12CA1CA9MMP1MMP2
SCHEMBL629569 0.77 CA12 (0.33) CA12CA1CA9MMP1MMP2
SCHEMBL150184 0.77 CA12 (0.33) CA12CA1CA9MMP1MMP2
SCHEMBL10953437 0.77 CA12 (0.39) CA12CA1CA9MMP1MMP2
SCHEMBL6005130 0.76 CA12 (0.32) CA12CA1CA9MMP1MMP2
SCHEMBL1400991 0.72 AKR1B1 (0.39) AKR1B1KDM5AKDM4CGPR84PPARG
SCHEMBL8253430 0.71 ZDHHC20 (0.42) AKR1B1GPR84PPARGPPARDPPARA

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 52 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119504500-A Synthesis process of propargyl butylcarbamate 安道麦安邦(江苏)有限公司 2025-02-25 CN claimed
US-20210337793-A1 ANTIMICROBIAL MIXTURES COMPRISING AT LEAST ONE HYDROXYPHENONE DERIVATIVE SYMRISE AG (DE) 2021-11-04 US claimed
CN-104704091-B The method for drying polyamidoimide film on threaded tubular component with high abrasion resistance is produced by the aqueous dispersion without carcinogen 瓦卢莱克油气法国公司 2017-03-08 CN claimed
EP-1651593-A4 PROCESS FOR THE SYNTHESIS OF IODOPROPYNYL BUTYLCARBAMATE IN AN AQUEOUS SOLUTION OF A SUITABLE SURFACTANT H & S CHEMICAL COMPANY INC (US) 2007-06-13 EP claimed
EP-1651593-A1 PROCESS FOR THE SYNTHESIS OF IODOPROPYNYL BUTYLCARBAMATE IN AN AQUEOUS SOLUTION OF A SUITABLE SURFACTANT H & S Chemical Company, Inc. (US) 2006-05-03 EP claimed
US-6992208-B2 Process for the synthesis of iodopropynyl butylcarbamate in an aqueous solution of a suitable surfactant H&S CHEMICAL COMPANY, INC. (US) 2006-01-31 US claimed
EP-1581052-A2 AN EMOLLIENT ALCOHOL SKIN DISINFECTING FORMULATION Becton, Dickinson and Company (US) 2005-10-05 EP claimed
WO-2005016871-A1 PROCESS FOR THE SYNTHESIS OF IODOPROPYNYL BUTYLCARBAMATE IN AN AQUEOUS SOLUTION OF A SUITABLE SURFACTANT H & S CHEMICAL COMPANY, INC. (US) 2005-02-24 WO claimed
US-20050033083-A1 Process for the synthesis of iodopropynyl butylcarbamate in an aqueous solution of a suitable surfactant FIRST FINANCIAL BANK 2005-02-10 US claimed
WO-2004062589-A2 AN EMOLLIENT ALCOHOL SKIN DISINFECTING FORMULATION BECTON DICKINSON AND COMPANY (US) 2004-07-29 WO claimed
US-5554784-A Process for preparing iodoalkynylcarbamates having a low tendency of yellowing when exposed to light GRUENING RAINER (US) 1996-09-10 US claimed
US-20250161202-A1 BIOME-FRIENDLY CONSUMER PRODUCTS AOBIOME LLC (US) 2025-05-22 US disclosed
CN-119504500-A Synthesis process of propargyl butylcarbamate 安道麦安邦(江苏)有限公司 2025-02-25 CN disclosed
US-12193441-B2 Antimicrobial mixtures comprising at least one hydroxyphenone derivative SYMRISE AG (DE) 2025-01-14 US disclosed
US-20240373845-A1 ANTIMICROBIAL MIXTURES COMPRISING AT LEAST ONE HYDROXYPHENONE DERIVATIVE SYMRISE AG (DE) 2024-11-14 US disclosed
EP-0814658-A4 FUNGICIDAL COMPOSITION ZENECA INC (US) 1999-02-17 EP disclosed
EP-0814658-A1 FUNGICIDAL COMPOSITION ZENECA INC. (US) 1998-01-07 EP disclosed
WO-1996028972-A1 FUNGICIDAL COMPOSITION ZENECA, INC. (US) 1996-09-26 WO disclosed
EP-0556518-B1 Impregnating waterproof composition SHINETSU CHEMICAL CO (JP) 1996-07-10 EP disclosed
US-4297258-A Non-yellowing paint formulations containing iodo substituted alkynyl urethanes as fungicides ICI AMERICAS INC. (US) 1981-10-27 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20240373845-A1 ANTIMICROBIAL MIXTURES COMPRISING AT LEAST ONE HYDROXYPHENONE DERIVATIVE HPD, GRHPR, ALDH7A1 CA12 3567/4885CA1 1926/4885CA9 3265/4885
US-12193441-B2 Antimicrobial mixtures comprising at least one hydroxyphenone derivative HOGA1, GNPAT, CLPP CA12 4785/4885CA1 4727/4885CA9 4770/4885
US-20210337793-A1 ANTIMICROBIAL MIXTURES COMPRISING AT LEAST ONE HYDROXYPHENONE DERIVATIVE HOGA1, GNPAT, CLPP CA12 4785/4885CA1 4727/4885CA9 4770/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.